Константинова Лидия Сергеевна

Константинова Лидия Сергеевна

Число
публикаций
Общее число
цитирований
Индекс
Хирша
86
1189
21
д.х.н.
Q2
Synthesis of 2-((2-(Benzo[d]oxazol-2-yl)-2H-imidazol -4-yl)amino)-phenols from 2-((5H-1,2,3-Dithiazol -5-ylidene)amino)phenols through Unprecedented Formation of Imidazole Ring from Two Methanimino Groups
Baranovsky I.V., Konstantinova L.S., Tolmachev M.A., Popov V.V., A. Lyssenko K., Rakitin O.A.
Molecules, 2020, цитирований: 1
Q4
Ethyl 11a,12-dihydrobenzo[b]benzo[5,6][1,4]oxazino[2,3-e][ 1,4]oxazine-5a(6h)-carboxylate
Konstantinova L.S., Tolmachev M.A., Popov V.V., Rakitin O.A.
MolBank, 2020, цитирований: 1
Q1
Progress in the chemistry of nitrogen-, oxygen- And sulfur-containing heterocyclic systems
Danilkina N.A., Vasileva A.A., Balova I.A.
Russian Chemical Reviews, 2020, цитирований: 2
Q2
Antimicrobial and antifungal activity of rare substituted 1,2,3-thiaselenazoles and corresponding matched pair 1,2,3-dithiazoles
Laitinen T., Baranovsky I.V., Konstantinova L.S., Poso A., Rakitin O.A., Asquith C.R.
Antibiotics, 2020, цитирований: 3
Q2
Synthesis and identification of pentathiepin-based inhibitors of sporothrix brasiliensis
Asquith C.R., Machado A.C., de Miranda L.H., Konstantinova L.S., Almeida-Paes R., Rakitin O.A., Pereira S.A.
Antibiotics, 2019, цитирований: 2
Q2
Synthesis and comparison of substituted 1,2,3-dithiazole and 1,2,3-thiaselenazole as inhibitors of the feline immunodeficiency virus (FIV) nucleocapsid protein as a model for HIV infection
Asquith C.R., Meili T., Laitinen T., Baranovsky I.V., Konstantinova L.S., Poso A., Rakitin O.A., Hofmann-Lehmann R.
Bioorganic and Medicinal Chemistry Letters, 2019, цитирований: 11
Q1
Investigation of the Pentathiepin Functionality as an Inhibitor of Feline Immunodeficiency Virus (FIV) via a Potential Zinc Ejection Mechanism, as a Model for HIV Infection
Asquith C.R., Laitinen T., Konstantinova L.S., Tizzard G., Poso A., Rakitin O.A., Hofmann‐Lehmann R., Hilton S.T.
ChemMedChem, 2019, цитирований: 6
Q2
Exploration and Development of a C-H-Activated Route to Access the [1,2]Dithiolo[4,3- b ]indole-3(4 H)-thione Core and Related Derivatives
Hilton S., Asquith C., Konstantinova L., Tizzard G., Laitinen T., Coles S., Rakitin O.
Synlett, 2019, цитирований: 3
Q3
Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release
Konstantinova L.S., Knyazeva E.A., Gatilov Y.V., Zlotin S.G., Rakitin O.A.
Russian Chemical Bulletin, 2018, цитирований: 7
Q2
The Conversion of 5,5-Bi(1,2,3-dithiazolylidenes) into Isothiazolo[5,4-d]isothiazoles
Konstantinova L., Baranovsky I., Strunyasheva V., Kalogirou A., Popov V., Lyssenko K., Koutentis P., Rakitin O.
Molecules, 2018, цитирований: 4
Q1
Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
Konstantinova L.S., Baranovsky I.V., Pritchina E.A., Mikhailov M.S., Bagryanskaya I.Y., Semenov N.A., Irtegova I.G., Salnikov G.E., Lyssenko K.A., Gritsan N.P., Zibarev A.V., Rakitin O.A.
Chemistry - A European Journal, 2017, цитирований: 14
Q3
Suzuki cross-coupling reactions of 4,7-dibromo[1, 2, 5]selenadiazolo[3,4-c]pyridine – a path to new solar cell components
Knyazeva E.A., Chmovzh T.N., Ustimenko O.O., Chkhetiani G.R., Paleva I.S., Konstantinova L.S., Mikhal’chenko L.V., Rakitin O.A.
Chemistry of Heterocyclic Compounds, 2017, цитирований: 5
Q1
New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
Chulanova E.A., Pritchina E.A., Malaspina L.A., Grabowsky S., Mostaghimi F., Beckmann J., Bagryanskaya I.Y., Shakhova M.V., Konstantinova L.S., Rakitin O.A., Gritsan N.P., Zibarev A.V.
Chemistry - A European Journal, 2017, цитирований: 19
Q4
Synthesis, crystal structure and electroluminescent properties of fac-bromotricarbonyl([1,2,5]oxadiazolo[3',4':5,6]pyrazino-[2,3-f][1,10]phenanthroline)rhenium (I)
Taydakov I.V., Vashchenko A.A., Lyssenko K.A., Konstantinova L.S., Knyazeva E.A., Obruchnikova N.V.
Arkivoc, 2017, цитирований: 3
Q3
Synthesis of 4-substituted 3-chloro-1,2,5-thiadiazoles from monosubstituted glyoximes
Kryshenko F.I., Knyazeva E.A., Konstantinova L.S., Rakitin O.A.
Russian Chemical Bulletin, 2016, цитирований: 4